Aberrant trafficking of a Leu89Pro connexin32 mutant associated with X-linked dominant Charcot–Marie–Tooth disease-Reference-Cited by-同舟云学术

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Aberrant trafficking of a Leu89Pro connexin32 mutant associated with X-linked dominant Charcot–Marie–Tooth disease

Published:2016-07-01 Issue:10 Volume:38 Page:897-902
ISSN:0161-6412
Container-title:Neurological Research
language:en
Short-container-title:Neurological Research

Author:

Da Yuwei¹,Wang Wei¹,Liu Zhongfeng²,Chen Hai¹,Di Li¹,Previch Lauren³,Chen Zhiguo²⁴

Affiliation:

1. Department of Neurology, Xuan Wu Hospital, Capital Medical University, Beijing, China

2. Cell Therapy Center, Xuan Wu Hospital, Capital Medical University, and Key Laboratory of Neurodegeneration, Ministry of Education, Beijing, China

3. Department of Neurological Surgery, Wayne State University School of Medicine, Taylor, MI, USA

4. Center of Neural Injury and Repair, Beijing Institute for Brain Disorders, Beijing, China

Funder

Beijing Natural Science Foundation Program and Scientific Research Key Program of Beijing Municipal Commission of Education

National Natural Science Funds

Publisher

Informa UK Limited

Subject

Clinical Neurology,Neurology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/01616412.2016.1204494

Reference30 articles.

1. Muscle & Nerve

2. Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

3. Connexin32 is a myelin-related protein in the PNS and CNS

4. Functional Gap Junctions in the Schwann Cell Myelin Sheath

5. The Gap Junction Communication Channel

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Whole Exome Sequencing Revealed a Novel GJB1 Pathogenic Variant and a Rare BSCL2 Mutation in Two Iranian Large Pedigrees with Multiple Affected Cases of Charcot-Marie-Tooth;INT J MOL CELL MED;2019

2. Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease;Human Molecular Genetics;2017-10-25

3. Cx32 inhibits TNFα-induced extrinsic apoptosis with and without EGFR suppression;Oncology Reports;2017-09-07

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